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{"title":"Synthesis, Characterization, and Function of an RNA-Based Transfection Reagent","authors":"Harsh V. Jain, Jessica F. Boehler, Kanneboyina Nagaraju, Serge L. Beaucage","doi":"10.1002/cpnc.51","DOIUrl":null,"url":null,"abstract":"<p>A synthetic 8-mer, amphipathic, <i>trans</i>-acting poly-2′-<i>O</i>-methyluridylic thiophosphate triester RNA element (2′-OMeUtaPS) can be prepared using solid-phase synthesis protocols. 2′-OMeUtaPS efficiently mediates the delivery of uncharged polyA-tailed phosphorodiamidate morpholino (PMO) sequences in HeLa pLuc 705 cells, as evidenced by flow cytometry measurements. In this cell line, 2′-OMeUtaPS-mediated transfection of an antisense polyA-tailed PMO sequence induces alternative splicing of an aberrant luciferase pre-mRNA splice site, leading to restoration of functional luciferase, as quantitatively measured using a typical luciferase assay. 2′-OMeUtaPS is also potent at delivering an uncharged antisense polyA-tailed PMO sequence in muscle cells of the <i>mdx</i> mouse model of muscular dystrophy; targeting the polyA-tailed PMO sequence against a splice site of the pre-mRNA encoding mutated dystrophin triggers an alternate splicing event that results in excision of the mutated exon (exon 23) from the pre-mRNA and production of functional dystrophin, as demonstrated by agarose gel electrophoresis. © 2018 by John Wiley & Sons, Inc.</p>","PeriodicalId":10966,"journal":{"name":"Current Protocols in Nucleic Acid Chemistry","volume":"72 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-04-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpnc.51","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Nucleic Acid Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpnc.51","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Chemistry","Score":null,"Total":0}
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Abstract
A synthetic 8-mer, amphipathic, trans -acting poly-2′-O -methyluridylic thiophosphate triester RNA element (2′-OMeUtaPS) can be prepared using solid-phase synthesis protocols. 2′-OMeUtaPS efficiently mediates the delivery of uncharged polyA-tailed phosphorodiamidate morpholino (PMO) sequences in HeLa pLuc 705 cells, as evidenced by flow cytometry measurements. In this cell line, 2′-OMeUtaPS-mediated transfection of an antisense polyA-tailed PMO sequence induces alternative splicing of an aberrant luciferase pre-mRNA splice site, leading to restoration of functional luciferase, as quantitatively measured using a typical luciferase assay. 2′-OMeUtaPS is also potent at delivering an uncharged antisense polyA-tailed PMO sequence in muscle cells of the mdx mouse model of muscular dystrophy; targeting the polyA-tailed PMO sequence against a splice site of the pre-mRNA encoding mutated dystrophin triggers an alternate splicing event that results in excision of the mutated exon (exon 23) from the pre-mRNA and production of functional dystrophin, as demonstrated by agarose gel electrophoresis. © 2018 by John Wiley & Sons, Inc.
一种基于RNA的转染试剂的合成、表征和功能。
可以使用固相合成方案制备合成的8聚体、两亲性、反式作用的聚2'-O-甲基脲基硫代磷酸三酯RNA元件(2'-OMeUtaPS)。流式细胞术测量证明,2'-OMeUtaPS有效介导HeLa pLuc 705细胞中不带电的聚A尾磷酸二酰胺吗啉(PMO)序列的递送。在该细胞系中,2'-OMeUtaPS介导的反义polyA尾PMO序列的转染诱导异常萤光素酶前mRNA剪接位点的选择性剪接,导致功能性萤光素酶的恢复,如使用典型萤光素酶测定法定量测量的。2'-OMeUtaPS在肌营养不良的mdx小鼠模型的肌肉细胞中也能有效地递送不带电的反义polyA尾PMO序列;如琼脂糖凝胶电泳所示,针对编码突变的肌营养不良蛋白的前mRNA的剪接位点靶向polyA尾PMO序列触发交替剪接事件,该交替剪接事件导致从前mRNA切除突变的外显子(外显子23)并产生功能性肌营养不良素。©2018 John Wiley&Sons,股份有限公司版权所有。
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